List of variants in gene NRXN1 reported as likely benign by Genetic Services Laboratory, University of Chicago

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 22

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HGVS	dbSNP	gnomAD frequency
NM_001330078.2(NRXN1):c.511C>T (p.Leu171=)	rs1045874	0.17452
NM_001330078.2(NRXN1):c.900C>T (p.Pro300=)	rs2303298	0.01844
NM_001330078.2(NRXN1):c.4068G>A (p.Thr1356=)	rs74714098	0.01437
NM_001330078.2(NRXN1):c.772+1140G>A	rs61658382	0.00837
NM_001330078.2(NRXN1):c.3408G>A (p.Thr1136=)	rs80094872	0.00737
NM_001330078.2(NRXN1):c.3249C>T (p.Pro1083=)	rs116236999	0.00578
NM_001330078.2(NRXN1):c.3933A>G (p.Ala1311=)	rs79970751	0.00503
NM_001330078.2(NRXN1):c.1285C>T (p.Pro429Ser)	rs78540316	0.00323
NM_001330078.2(NRXN1):c.4473G>A (p.Ala1491=)	rs113380721	0.00191
NM_001330078.2(NRXN1):c.501C>G (p.Leu167=)	rs200248561	0.00145
NM_001330078.2(NRXN1):c.222C>T (p.Gly74=)	rs201592993	0.00135
NM_001330078.2(NRXN1):c.3045C>T (p.Ala1015=)	rs56402642	0.00109
NM_001330078.2(NRXN1):c.4254A>G (p.Pro1418=)	rs55923848	0.00109
NM_001330078.2(NRXN1):c.1158+26A>T	rs201802152	0.00069
NM_001330078.2(NRXN1):c.1365T>C (p.Leu455=)	rs201727684	0.00051
NM_001330078.2(NRXN1):c.4392T>C (p.His1464=)	rs112536447	0.00035
NM_001330078.2(NRXN1):c.1050C>G (p.Ala350=)	rs201397488	0.00010
NM_001330078.2(NRXN1):c.3090A>C (p.Gly1030=)	rs201886024	0.00010
NM_001330078.2(NRXN1):c.2211G>A (p.Thr737=)	rs755177932	0.00002
NM_001330078.2(NRXN1):c.1326A>C (p.Val442=)	rs201485014	0.00001
NM_001330078.2(NRXN1):c.3009A>T (p.Val1003=)	rs781048514
NM_001330078.2(NRXN1):c.3192C>T (p.Asp1064=)	rs199580594

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